Public Citizen v. Department of Health & Human Services

795 F. Supp. 1212, 1992 U.S. Dist. LEXIS 8188, 1992 WL 128424
CourtDistrict Court, District of Columbia
DecidedMay 28, 1992
DocketCiv. A. 92-0326
StatusPublished
Cited by11 cases

This text of 795 F. Supp. 1212 (Public Citizen v. Department of Health & Human Services) is published on Counsel Stack Legal Research, covering District Court, District of Columbia primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Public Citizen v. Department of Health & Human Services, 795 F. Supp. 1212, 1992 U.S. Dist. LEXIS 8188, 1992 WL 128424 (D.D.C. 1992).

Opinion

MEMORANDUM OPINION

THOMAS F. HOGAN, District Judge.

This case is brought by Public Citizen, the National Resources Defense Council, the Center for Science in the Public Interest, and the California Environmental Protection Agency’s Office of Environmental Health Hazard Assessment against the Department of Health and Human Services (HHS) for the alleged violation of the Federal Advisory Committee Act (FACA), 5 U.S.C.App. § 5(b)(2) & (c). Before the Court are defendant’s motion to dismiss and plaintiffs’ cross motion for summary judgment. For the reasons that follow, this Court shall grant defendant’s motion and deny plaintiffs’ motion and dismiss this case.

*1213 BACKGROUND

The material facts are not in dispute. On November 20, 1989, the Secretary of HHS, Louis Sullivan, chartered the Advisory Committee on the Food and Drug Administration (FDA Advisory Committee or the Committee) for the purpose of examining “the mission, responsibilities and structure of the FDA according to its legislative mandate and to make recommendations on how the Agency can be strengthened to fulfill its mission.”. See Plaintiffs’ Exhibit 21 (Charter of the Advisory Committee on the Food and Drug Administration) (hereinafter Charter). The Committee was originally structured to have 13 members appointed by the Secretary. On April 4, 1990, the Secretary amended the Charter to add four members and give the Committee additional time to accomplish its assigned tasks. The Charter expired just over a year later, with the issuance of the Committee’s May 1991 Final Report. See Plaintiffs’ Exhibit 30 (Final Report of the Advisory Committee on the Food and Drug Administration, May 1991) (hereinafter Final Report).

Plaintiffs’ complaint takes issue with one of the recommendations in the final report: the recommendation that Congress pass legislation preempting additional and conflicting state requirements for all products subject to FDA jurisdiction. The Committee’s recommendation includes a procedure whereby states may seek exemption from preemption in areas in which the FDA has acted, based on “convincing local need.” Additionally, the recommendation provides that in areas in which the FDA has not acted, a state that wishes to act must notify the FDA and give it 120 days to respond. Finally, the recommendation provides that states should be allowed to petition for the adoption or amendment of national standards. The FDA Advisory Committee additionally recommended that if Congress does not pass preemption legislation by the end of the 102nd Congress, then the FDA should issue a preemption regulation accomplishing the same goals. See Final Report at 49-53.

Plaintiffs argue that the FDA Advisory Committee acted ultra vires by making the preemption recommendation because the Committee is not “fairly balanced in terms of the points of view represented and the functions to be performed,” as required by the FACA, 5 U.S.C.App. § 5(b)(2) & (c). Plaintiffs argue that in order for the Committee to make a recommendation involving states’ rights and interests, the FACA requires that the Committee include representatives of states’ interests. The FDA Advisory Committee allegedly contains no such members. 1 Thus, plaintiffs seek a declaration that the Committee’s recommendation regarding preemption is null and void. They also seek an injunction requiring HHS to amend the Final Report to delete the recommendation and to notify those who have received copies that the recommendation has been deleted.

The government advances three arguments in support of its motion to dismiss: (1) that plaintiffs’ claim is nonjusticiable because of the lack of a judicially manageable standard of review of the “fair balance” requirement; (2) that plaintiffs lack standing to pursue their claim; and (3) that, on the merits, the Secretary did not abuse his appointment discretion in appointing the members of the FDA Advisory Committee.

DISCUSSION

A. The Case. Law

The FACA “fair balance” requirement has been addressed by this circuit on four occasions (and more frequently by the district court). Unfortunately, the decisions that have been rendered thus far have resulted in a legal quagmire with no coherent guidelines for district courts to follow.

The first case to address the issue was Metcalf v. Nat’l Petroleum Council, 553 F.2d 176 (D.C.Cir.1977) (Wilkey, J., writing *1214 for Tamm & MacKinnon, J.J.). In that case, a U.S. senator, Lee Metcalf, and a private citizen, Robert Brown, brought suit to enjoin the National Petroleum Council (NPC) from operating as a federal advisory committee because its membership allegedly was not “fairly balanced” within the requirements of the FACA. Specifically, plaintiffs alleged that the NPC, made up entirely of petroleum industry representatives, was inappropriately influenced by special interests. Judge Pratt dismissed the case for lack of standing and the circuit court affirmed.

In Metcalf, the private citizen argued that citizens and consumers were injured by the NPC’s composition because, as a result of the influence of the petroleum industry, the NPC would make recommendations that would result in higher prices for petroleum products, a lack of policy interest in alternative energy sources,, and a threat to citizens’ health and safety because of the environmental damage associated with petroleum products. The circuit court held that these alleged injuries did not rise to the “injury in fact” required for standing because “the occurrence of the asserted harm is speculative and conjectural in the purest sense.” 553 F.2d at 186. Plaintiffs’ own allegations mandated this conclusion: their claims rested on the theory that the unbalanced membership of the NPC “causes it to make certain biased recommendations, which in turn cause government agencies to adopt policies favoring the petroleum industry, which in turn cause the appellants to be injured as consumers and citizens.” Id. at 185. This speculative chain of events was simply too attenuated to amount to injury in fact.

The circuit court reached the same conclusion with respect to the alleged injuries of Senator Metcalf. He argued that, as a member of the Senate Committee on Interi- or and Insular Affairs and Chairman of its Subcommittee on Minerals, Materials and Fuels, the subcommittee’s work suffered because of the allegedly tainted and biased advice of the NPC. The court held that the senator had “alleged no ‘particular concrete injury’ which amounts to ‘a claim of specific present objective harm or a threat of specific future harm.’ ” Id. at 188 (citations omitted) (emphasis in original). Rather, he presented only a generalized grievance that one of the sources of information to the subcommittee was not of the quality it should be.

Finally, in affirming the district court’s dismissal of the case; the circuit stated:

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Bluebook (online)
795 F. Supp. 1212, 1992 U.S. Dist. LEXIS 8188, 1992 WL 128424, Counsel Stack Legal Research, https://law.counselstack.com/opinion/public-citizen-v-department-of-health-human-services-dcd-1992.